Incidental Mutation 'R7452:Cyp4a12a'
ID577791
Institutional Source Beutler Lab
Gene Symbol Cyp4a12a
Ensembl Gene ENSMUSG00000066071
Gene Namecytochrome P450, family 4, subfamily a, polypeptide 12a
SynonymsCyp4a12
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.084) question?
Stock #R7452 (G1)
Quality Score225.009
Status Validated
Chromosome4
Chromosomal Location115299046-115332815 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 115327598 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 359 (I359F)
Ref Sequence ENSEMBL: ENSMUSP00000081370 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084343]
Predicted Effect probably damaging
Transcript: ENSMUST00000084343
AA Change: I359F

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000081370
Gene: ENSMUSG00000066071
AA Change: I359F

DomainStartEndE-ValueType
low complexity region 18 39 N/A INTRINSIC
Pfam:p450 51 503 1e-131 PFAM
Meta Mutation Damage Score 0.6406 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 98.8%
Validation Efficiency 100% (75/75)
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406P16Rik A G 7: 34,245,671 S595P probably benign Het
A2m C A 6: 121,641,332 Q195K probably damaging Het
Abcg4 C T 9: 44,279,600 G249R probably damaging Het
Actn1 T C 12: 80,183,602 T293A probably benign Het
Adamts5 T A 16: 85,877,981 T432S probably benign Het
Adh5 A G 3: 138,454,745 T347A probably benign Het
Agbl5 A G 5: 30,893,391 D432G probably damaging Het
Ank3 A G 10: 69,899,051 T797A possibly damaging Het
Aoc1 T G 6: 48,908,790 V743G probably benign Het
Arap2 A T 5: 62,676,549 S858R probably benign Het
Arid1a A C 4: 133,753,127 V162G possibly damaging Het
Armc9 A G 1: 86,213,092 D588G possibly damaging Het
Art3 A G 5: 92,392,680 Y94C probably damaging Het
Btaf1 T A 19: 36,969,127 D444E probably damaging Het
Cav2 A G 6: 17,282,076 H111R probably damaging Het
Ccdc148 A G 2: 58,827,584 L469P probably damaging Het
Celsr2 T A 3: 108,413,090 E802V possibly damaging Het
Cfap57 T C 4: 118,595,784 D574G probably damaging Het
Chd7 A C 4: 8,854,731 D2024A probably benign Het
Corin T A 5: 72,435,247 D269V possibly damaging Het
Defb6 T C 8: 19,225,524 L7P probably damaging Het
Dnah7c A T 1: 46,647,036 M1817L possibly damaging Het
Dock3 A G 9: 106,989,465 F682S probably damaging Het
Enpep T A 3: 129,271,403 Y879F possibly damaging Het
Enpp2 T C 15: 54,866,736 N462S probably damaging Het
Ephb3 T C 16: 21,217,357 probably null Het
F7 C T 8: 13,035,215 H414Y probably benign Het
Fbn1 T C 2: 125,505,455 H50R possibly damaging Het
Fig4 T C 10: 41,240,637 D586G possibly damaging Het
Fryl A G 5: 73,023,988 L2825P probably damaging Het
Gal3st2 T A 1: 93,872,518 H30Q possibly damaging Het
Gm12886 G A 4: 121,417,474 Q70* probably null Het
Gm8104 A C 14: 43,110,044 T190P probably benign Het
Hps3 A T 3: 20,011,428 N749K probably damaging Het
Hr A G 14: 70,571,486 T1101A probably damaging Het
Htatip2 T A 7: 49,773,326 S210T probably benign Het
Ift80 T C 3: 68,994,282 probably null Het
Iqgap1 A G 7: 80,760,829 V212A possibly damaging Het
Itih5 A G 2: 10,238,796 E448G probably damaging Het
Kdm5b T C 1: 134,624,948 C1221R probably damaging Het
Lrrc72 T C 12: 36,212,693 Y52C probably benign Het
Map1b C T 13: 99,508,140 R85Q probably damaging Het
Mdn1 T C 4: 32,739,030 I3617T possibly damaging Het
Mtpap T A 18: 4,379,705 H98Q possibly damaging Het
Nemf A T 12: 69,337,959 probably null Het
Neto1 A T 18: 86,498,931 I458L probably benign Het
Nfam1 T A 15: 83,014,962 M128L probably benign Het
Olfr1279 A G 2: 111,306,921 T239A probably damaging Het
Olfr1383 C A 11: 49,524,381 H219Q probably benign Het
Olfr501-ps1 C T 7: 108,508,593 T179I unknown Het
Olfr914 A T 9: 38,607,088 I208F probably benign Het
P2ry14 C T 3: 59,116,045 G7D probably benign Het
Pde11a A G 2: 76,136,414 Y564H probably damaging Het
Pex5l C T 3: 33,004,318 V262I probably benign Het
Poli A G 18: 70,508,978 V717A possibly damaging Het
Prdm14 A T 1: 13,125,559 W93R probably damaging Het
Rbm46 T C 3: 82,864,121 M396V probably benign Het
Rcor2 T C 19: 7,271,222 V212A probably benign Het
Rcor3 C A 1: 192,137,876 G8V probably damaging Het
Rhox4d G A X: 37,518,992 G191E unknown Het
Rictor C T 15: 6,772,154 S441L probably benign Het
Skp2 T A 15: 9,113,832 Q366L probably damaging Het
Slc13a3 A T 2: 165,427,114 S312T probably benign Het
Sstr1 T C 12: 58,213,356 L255P probably damaging Het
Steap3 T C 1: 120,227,855 E458G possibly damaging Het
Sv2b T A 7: 75,147,713 D311V probably damaging Het
Tmem132b A G 5: 125,638,268 D347G probably benign Het
Tmem161a A G 8: 70,177,488 D108G probably damaging Het
Traf5 T A 1: 191,999,831 I47F Het
Trp53bp2 C T 1: 182,446,568 Q95* probably null Het
Ttn G T 2: 76,877,143 probably null Het
Usf3 T C 16: 44,220,034 S1626P probably benign Het
Usp3 T C 9: 66,566,898 R33G probably benign Het
Zbtb20 G T 16: 43,610,676 A517S probably damaging Het
Other mutations in Cyp4a12a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00931:Cyp4a12a APN 4 115301956 missense possibly damaging 0.87
IGL00948:Cyp4a12a APN 4 115301962 missense probably damaging 0.98
IGL03143:Cyp4a12a APN 4 115302003 missense probably benign 0.00
R0099:Cyp4a12a UTSW 4 115326672 missense probably damaging 1.00
R0371:Cyp4a12a UTSW 4 115326683 missense probably damaging 0.97
R1893:Cyp4a12a UTSW 4 115326667 missense probably benign 0.03
R2018:Cyp4a12a UTSW 4 115327505 missense probably damaging 1.00
R3423:Cyp4a12a UTSW 4 115327274 missense probably benign 0.37
R4445:Cyp4a12a UTSW 4 115326783 critical splice donor site probably null
R4586:Cyp4a12a UTSW 4 115327312 missense probably benign 0.01
R4765:Cyp4a12a UTSW 4 115326191 missense possibly damaging 0.95
R4823:Cyp4a12a UTSW 4 115327413 critical splice acceptor site probably null
R5131:Cyp4a12a UTSW 4 115327820 missense possibly damaging 0.60
R5841:Cyp4a12a UTSW 4 115326702 missense probably benign 0.03
R6017:Cyp4a12a UTSW 4 115326279 nonsense probably null
R6039:Cyp4a12a UTSW 4 115327223 missense probably damaging 1.00
R6039:Cyp4a12a UTSW 4 115327223 missense probably damaging 1.00
R6170:Cyp4a12a UTSW 4 115327446 missense possibly damaging 0.60
R6883:Cyp4a12a UTSW 4 115302024 missense probably damaging 1.00
R7308:Cyp4a12a UTSW 4 115327758 missense possibly damaging 0.60
R7327:Cyp4a12a UTSW 4 115327559 missense probably damaging 1.00
R7595:Cyp4a12a UTSW 4 115331892 missense probably damaging 1.00
R7638:Cyp4a12a UTSW 4 115327473 missense possibly damaging 0.93
R8040:Cyp4a12a UTSW 4 115326215 missense probably benign 0.12
R8303:Cyp4a12a UTSW 4 115328933 missense probably damaging 1.00
X0024:Cyp4a12a UTSW 4 115327812 missense probably benign 0.39
Z1176:Cyp4a12a UTSW 4 115329003 critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- GCGACTTGACCTAGAACCAGAG -3'
(R):5'- TGGTACAGGAGGGTAGATCC -3'

Sequencing Primer
(F):5'- CTCATCTGTGGTCTTATCCAGATGG -3'
(R):5'- GTAGATCCTCAGGGCCTCCTTG -3'
Posted On2019-10-07